Acids & Bases Flashcards
What are the causal/ “maintenance” mechanisms of a renal metabolic alkalosis?
- Volume contraction- causes proximal HCO3 reabsorption with sodium
- Hypokalemia (from increased aldosterone activity) causes an increase in acid excretion
Gitelman’s syndrome
Autosomal recessive condition, resembles action of a thiazide diuretic
Renal electrolyte wasting with metabolic alkalosis
may have osmotic diuresis from ions
Bartter’s Syndrome
Resembles loop diuretic, causes decreased EABV and excretion of sodium, potassium, chloride
Usually picked up early in life
Positive urine charge
This results from issues with ammonium secretion- not as much chlorine goes out so less negative charges in the urine
Negative urine charge
This means that ammonium secretion is normal, and there is lots of chlorine in the urine so net negative
RTA I
Alpha cell issue with ammonium secretion
Causes: secretory defect
clues: positive urine charge, high TTKG
RTA II
PCT issue with bicarb reabsorption
clues: negative urine charge, high Fe HCO3
RTA IV
Principal cell issue with ammonium secretion
causes: hyperkalemia causing defective ammoniagenesis or low NH3 availability
clues: positive urine charge, low TTKG
What is required for H+ secretion in ammonium?
- Proton pump
- Luminal negative charge
- NH3
Where and how is H+ secreted?
- Cortical collecting duct as:
Sodiumphosphate
Ammonium chloride
Where is bicarb reabsorbed?
The PCT
Salicylate poisoning
Acidemia but may have compensating respiratory alkalosis
May have hypokalemia
Normal compensation for metabolic acidosis
1:1
Normal compensation for metabolic alkalosis
10:7